CCL17 influences Borrelia burgdorferi infection in the heart

Xiaotian Tang, Qian Yu, Yingjun Cui, Thomas M Hart, Freddie Rivas-Giorgi, Keith Calloway, Amrita Ray Mohapatra, Erol Fikrig
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Abstract

Lyme disease, caused by Borrelia burgdorferi, is transmitted to humans by Ixodes ticks. CCL17 is a potent chemokine that plays important roles in diverse illnesses, including autoimmune and infectious diseases. CCL17 knockout (KO) mice, infected with B. burgdorferi, had a reduced pathogen load in the heart, compared to control animals. Mice lacking CCL17 also showed signs of immune alteration upon B. burgdorferi infection, including diverse serum levels of proinflammatory cytokines and fewer monocytes and macrophages infiltration. CCL17 also interacts directly with B. burgdorferi, the first demonstration that this chemokine has an affinity for a vector-borne pathogen.
CCL17对心脏伯氏疏螺旋体感染的影响
由伯氏疏螺旋体引起的莱姆病通过蜱虫传播给人类。CCL17是一种有效的趋化因子,在多种疾病中发挥重要作用,包括自身免疫性疾病和传染病。与对照动物相比,感染伯氏疏螺旋体的CCL17敲除(KO)小鼠心脏中的病原体负荷减少。缺乏CCL17的小鼠在伯氏疏螺旋体感染后也表现出免疫改变的迹象,包括血清促炎细胞因子水平不同,单核细胞和巨噬细胞浸润减少。CCL17还直接与伯氏疏螺旋体相互作用,这是首次证明该趋化因子与媒介传播的病原体具有亲和力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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